Lafitte G, Thuresson K, Jarwoll P, Nydén M
Physical Chemistry 1, Center for Chemistry and Chemical Engineering, Lund University, P.O. Box 124, SE-221 00 Lund, Sweden.
Langmuir. 2007 Oct 23;23(22):10933-9. doi: 10.1021/la701081s. Epub 2007 Sep 26.
The aqueous environment in the gastrointestinal tract frequently requires solubilization of hydrophobic drug molecules in appropriate drug delivery vehicles. An effective uptake/absorption and systemic exposure of a drug molecule entails many processes, one being transport properties of the vehicles through the mucus layer. The mucus layer is a complex mixture of biological molecules. Among them, mucin is responsible of the gel properties of this layer. In this study, we have investigated the diffusion of polyoxyethylene sorbitane monooleate (polysorbate 80), a commonly used nonionic surfactant, in aqueous solution, in mucin solutions at 0.25 and 5 wt %, and in mucus. These measurements were done by using the pulsed field gradient spin echo nuclear magnetic resonance (PGSE-NMR) technique. We conclude that polysorbate 80 is a mixture of non-surface-active molecules that can diffuse freely through all the systems investigated and of surface-active molecules that form micellar structures with transport properties strongly dependent on the environment. Polysorbate 80 micelles do not interact with mucin even though their diffusion is hindered by obstruction of the large mucin molecules. On the other hand, the transport is slowed down in mucus due to interactions with other components such as lipids depots. In the last part of this study, a hydrophobic NMR probe molecule has been included in the systems to mimic a hydrophobic drug molecule. The measurements done in aqueous solution revealed that the probe molecules were transported in a closely similar way as the polysorbate 80 micelles, indicating that they were dissolved in the micellar core. The situation was more complex in mucus. The probe molecules seem to dissolve in the lipid depots at low concentrations of polysorbate 80, which slows down their transport. At increasing concentration of polysorbate 80, the diffusion of the probe molecules increases indicating a continuous dissolution of hexamethyldisilane in the core of polysorbate 80 micelles.
胃肠道中的水性环境常常需要将疏水性药物分子溶解在合适的药物递送载体中。药物分子的有效摄取/吸收和全身暴露需要许多过程,其中之一是载体通过黏液层的转运特性。黏液层是生物分子的复杂混合物。其中,黏蛋白决定了该层的凝胶特性。在本研究中,我们研究了常用的非离子表面活性剂聚氧乙烯山梨醇酐单油酸酯(吐温80)在水溶液、0.25 wt%和5 wt%的黏蛋白溶液以及黏液中的扩散情况。这些测量是通过使用脉冲场梯度自旋回波核磁共振(PGSE-NMR)技术进行的。我们得出结论,吐温80是由非表面活性分子和表面活性分子组成的混合物,非表面活性分子可在所有研究的体系中自由扩散,表面活性分子形成胶束结构,其转运特性强烈依赖于环境。吐温80胶束即使扩散受到大的黏蛋白分子阻碍也不与黏蛋白相互作用;另一方面,由于与脂质库等其他成分相互作用,其在黏液中的转运减慢。在本研究的最后部分,在体系中加入了一种疏水性核磁共振探针分子以模拟疏水性药物分子。在水溶液中进行的测量表明探针分子的转运方式与吐温80胶束非常相似,这表明它们溶解在胶束核心中。在黏液中的情况更为复杂。在吐温80浓度较低时,探针分子似乎溶解在脂质库中,这减慢了它们的转运。随着吐温80浓度增加,探针分子的扩散增加,表明六甲基二硅烷在吐温80胶束核心中持续溶解。